FdaApplication

NDA 020199

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Identifiers

Properties

PropertyValue
applicant_nameHOFFMANN LA ROCHE INC
application_typeNDA
approval_date1992-06-19

Products (2)

ProductActive ingredientStrengthDosage form
HIVIDZALCITABINE0.75MGTABLET;ORAL
HIVIDZALCITABINE0.375MGTABLET;ORAL

2 products